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4320005: Factor V deficiency (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
780184015 Factor V deficiency (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
8280018 Factor V deficiency en Synonym Active Initial character case insensitive SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Factor V deficiency Interprets Haemostatic function true Inferred relationship Some 1
Factor V deficiency Has interpretation Abnormal true Inferred relationship Some 1
Factor V deficiency Is a Coagulation factor deficiency syndrome true Inferred relationship Some
Factor V deficiency Finding site Body system structure false Inferred relationship Some
Factor V deficiency Has definitional manifestation Haemostatic system finding false Inferred relationship Some
Factor V deficiency Finding site Entire haematological system false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Acquired factor V deficiency disease Is a True Factor V deficiency Inferred relationship Some
Hereditary factor V deficiency disease Is a True Factor V deficiency Inferred relationship Some
Combined deficiency of factor V and factor VIII Is a True Factor V deficiency Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

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